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Prospective Evaluation of Near and Intermediate Visual Outcomes With Monofocal Intraocular Lenses: The Mast Study

I

Innovative Medical

Status

Unknown

Conditions

Patients Implanted With Monofocal Intraocular Lens

Treatments

Device: Monofocal Intraocular Lenses

Study type

Observational

Funder types

Industry

Identifiers

NCT01191515
The Mast Study

Details and patient eligibility

About

The purpose of this study is to evaluate the near and intermediate visual outcomes of patients who have undergone routine cataract surgery (removal of cloudy crystalline lens) with phacoemulsification (the break-up and removal of cloudy lens) and monofocal IOL ( a plastic lens implanted to replace eye's natural lens) placement in the capsular bag in at least one eye.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Male or female patients at least 18 years of age
  • Patients who underwent routine cataract surgery with phacoemulsification and monofocal iol placement in the capsular bag in at least one eye within the last 36 months
  • At least 1 month postop before follow-up evaluation
  • All Patients must have a DCVA of 20/25 or better

Trial design

200 participants in 2 patient groups

Near visual outcomes with Monofocal IOL
Description:
Evaluation of intermediate visual outcomes of patients undergoing routine cataract surgery with phacoemulsification and monofocal IOl placement in the capsular bag in at least one eye.
Treatment:
Device: Monofocal Intraocular Lenses
Intermediate Visual outcomes
Description:
Evaluation of intermediate visual outcomes of patients undergoing routine cataract surgery with phacoemulsification and monofocal IOl placement in the capsular bag in at least one eye.
Treatment:
Device: Monofocal Intraocular Lenses

Trial contacts and locations

1

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Central trial contact

Jennifer Piel

Data sourced from clinicaltrials.gov

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